A case of marginal zone B cell lymphoma mimicking IgG4-related dacryoadenitis and sialoadenitis

نویسندگان

  • Miho Ohta
  • Masafumi Moriyama
  • Yuichi Goto
  • Shintaro Kawano
  • Akihiko Tanaka
  • Takashi Maehara
  • Sachiko Furukawa
  • Jun-Nosuke Hayashida
  • Tamotsu Kiyoshima
  • Mayumi Shimizu
  • Yojiro Arinobu
  • Seiji Nakamura
چکیده

BACKGROUND IgG4-related dacryoadenitis and sialoadenitis (IgG4-DS), so-called Mikulicz's disease, is characterized by elevated serum IgG4 and infiltration of IgG4-positive plasma cells in glandular tissues. Recently, several studies reported both malignant lymphoma developed on the background of IgG4-associated conditions and IgG4-producing malignant lymphoma (non-IgG4-related disease). CASE PRESENTATION We report on the case of a 70-year-old man who was strongly suspected IgG4-DS because of high serum IgG4 concentration (215 mg/dl) and bilateral swelling of parotid and submandibular glands. Biopsies of cervical lymph node and a portion of submandibular gland were performed. These histopathological findings subsequently confirmed a diagnosis of marginal zone B cell lymphoma. CONCLUSION Differential diagnosis of IgG4-DS is necessary from other disorders, including Sjögren's syndrome, sarcoidosis, Castleman's disease, Wegener's granulomatosis, lymphoma, and cancer. We suggest that biopsy of swollen lesions is important for a definitive diagnosis of IgG4-DS and discuss the mechanism of development in this case.

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عنوان ژورنال:

دوره 13  شماره 

صفحات  -

تاریخ انتشار 2015